Lead Medical Director CVRM/Heart Failure

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Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development clinical strategies and plans that deliver medically differentiated therapies that provide meaningful improvement to patients. 

Roche is looking for an experienced and highly specialized individual to join the Cardiovascular, Renal, and Metabolism group. The role of the Lead or Senior Medical Director will focus on guiding and shaping our cardiovascular outcomes strategy. To be successful in this role, you will need to have extensive experience in late stage drug development and managing large-scale clinical trials, including outcome studies, in particular we are looking for candidates with experience in heart failure programs.

You will have strong collaboration with cross-functional teams, including clinical research, regulatory affairs, and medical affairs, to ensure the successful progression of treatments through the pipeline and into the market. The position would also require a strong understanding of cardiovascular diseases, clinical trial protocols, regulatory requirements, and possibly interactions with regulatory agencies to ensure studies meet the required standards. 

You will interact with high level management and experts both internally and externally, serving as internal consultants

• You are expected to provide critical insights and contributions to the development and effectiveness of the assigned project

•  You have demonstrated a high level of experience in Clinical Development Plan (CDP) Strategy & Planning, Execution, Regulatory Activities, and Cross-Functional Team work/matrix leadership.

• You will mentor other physicians / scientists in their disease area of expertise as required.

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• You have an MD (board certified in Cardiology is preferred); along with significant clinical trial/late stage development experience in CVRM studies. Minimum 5+ years of pharma/biotech R&D experience

• You have experience authoring global trial plans and working with various health authorities as well as an understanding of how to run a large CV outcome trial. You have championed novel/innovative approaches to clinical development (i.e. study design, endpoints, technology)

• You have a strong external network with relevant experts for CVOTs.

• You have regulatory experience: providing clinical science information and input for regulatory submissions and other regulatory process

• You have the ability to collaborate with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in PD, research, business development, commercial operations, legal, etc, resulting in demonstrable outcomes

• You have strong interpersonal skills: outstanding interpersonal, verbal, and written communication and influencing skills: have built and cultivated important relationships both inside and outside of Roche; have proven abilities to influence internal partners and stakeholders, thought leaders, national advocacy  organizations, national standard-setting bodies, and other relevant external parties

If you are a Cardiologist with experience in Heart Failure Clinical Programs, we would love to hear from you.

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Roche is an Equal Opportunity Employer.